# K051366: Piconibp Oem Module

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medizin Systeme Boeblingen GmbH
- Decided: Sep 14, 2005 after 112 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K941811 (1994). 36 ancestors in all.
10 later devices descend from it; 1 cites it directly.
0 of 47 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020531: Philips Multi-Parameter Module, Model M3001A; Philips Component Compact Monitor, Release a.02, Model M1275B, Philips Medical Systems (2002) Summary page 1.
- K001333: Agilent Component Monitoring System, Agilent Multi-Measurement Server and Compact Portable Patient Monitor, Agilent Noni, Agilent Technologies Deutschland GmbH (2000) Summary page 1.
- K954351: Series 50XM, Hewlett-Packard GmbH (1996) Summary page 1.

## Most influential descendants
- K052795: Philips Avalon Fetal Monitor, Models FM20 and FM30 (2005), 9 descendants of its own
- K062137: Modification to Philips Avalon Fetal Monitors FM20 and FM30 (2006), 8 descendants of its own
- K071800: Philips Avalon Fetal Monitors FM20 and FM30 (2007), 7 descendants of its own
- K100420: Philips Obtracevue Model SW Rev. G.00 (2010), 4 descendants of its own
- K092028: Philips Avalon Fetal Monitors FM20, FM30, FM40, and FM50 (2010), 3 descendants of its own

## Indications for use
Indicated for use by health care professionals whenever there is a need for measuring the non-invasive blood pressure and pulse rate of patients. It is intended for use in patient monitors for measurement of blood pressure and for calculation of pulse rate of adults, pediatrics, and neonates in health care facilities.

Source page: https://510kreport.com/device/K051366
Methodology: https://510kreport.com/methodology